Canonical Allele Identifier: PA2825297089
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3075276
ClinVar RCV Id: RCV004015802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Thr2176Ser
CA362694915
NM_001008844.3:c.6526A>T
CA362694917
NM_001008844.3:c.6527C>G